Product Details

SNP ID

rs73116712

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:74795709 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTTCTATAAGGTAGATCTTATATC[A/T]TTTGTGTATGTAAGTGTGTTTAATT

Phenotype

MIM: 615769

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM169A PubMed Links

Gene Details

Gene

FAM169A

Gene Name

family with sequence similarity 169 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015566.2		Intron			NP_056381.1
XM_005248480.2		Intron			XP_005248537.1
XM_011543306.2		Intron			XP_011541608.1
XM_011543307.2		Intron			XP_011541609.1
XM_017009332.1		Intron			XP_016864821.1
XM_017009333.1		Intron			XP_016864822.1

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